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Zfp281 and Zfp148 control CD4+ T cell thymic development and TH2 functions.
Chopp, Laura B; Zhu, Xiaoliang; Gao, Yayi; Nie, Jia; Singh, Jatinder; Kumar, Parimal; Young, Kelly Z; Patel, Shil; Li, Caiyi; Balmaceno-Criss, Mariah; Vacchio, Melanie S; Wang, Michael M; Livak, Ferenc; Merchant, Juanita L; Wang, Lie; Kelly, Michael C; Zhu, Jinfang; Bosselut, Rémy.
Afiliação
  • Chopp LB; Laboratory of Immune Cell Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
  • Zhu X; Immunology Graduate Group, University of Pennsylvania Medical School, Philadelphia, PA 19104, USA.
  • Gao Y; Molecular and Cellular Immunoregulation Section, Laboratory of Immune System Biology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
  • Nie J; Laboratory of Immune Cell Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
  • Singh J; Laboratory of Immune Cell Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
  • Kumar P; Single Cell Analysis Facility, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
  • Young KZ; Single Cell Analysis Facility, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
  • Patel S; Department of Neurology, University of Michigan, Ann Arbor, MI 48109, USA.
  • Li C; Laboratory of Immune Cell Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
  • Balmaceno-Criss M; University of Maryland Medical School, Baltimore, MD 21201, USA.
  • Vacchio MS; Flow Cytometry Core, Laboratory of Genomic Integrity, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
  • Wang MM; Laboratory of Immune Cell Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
  • Livak F; Laboratory of Immune Cell Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
  • Merchant JL; Department of Neurology, University of Michigan, Ann Arbor, MI 48109, USA.
  • Wang L; Neurology Service, VA Ann Arbor Healthcare System, Ann Arbor, MI 48105, USA.
  • Kelly MC; Flow Cytometry Core, Laboratory of Genomic Integrity, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
  • Zhu J; Department of Gastroenterology and Hepatology, University of Arizona College of Medicine, Tucson, AZ 85724, USA.
  • Bosselut R; Institute of Immunology, and Bone Marrow Transplantation Center, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Sci Immunol ; 8(89): eadi9066, 2023 11 10.
Article em En | MEDLINE | ID: mdl-37948511
ABSTRACT
How CD4+ lineage gene expression is initiated in differentiating thymocytes remains poorly understood. Here, we show that the paralog transcription factors Zfp281 and Zfp148 control both this process and cytokine expression by T helper cell type 2 (TH2) effector cells. Genetic, single-cell, and spatial transcriptomic analyses showed that these factors promote the intrathymic CD4+ T cell differentiation of class II major histocompatibility complex (MHC II)-restricted thymocytes, including expression of the CD4+ lineage-committing factor Thpok. In peripheral T cells, Zfp281 and Zfp148 promoted chromatin opening at and expression of TH2 cytokine genes but not of the TH2 lineage-determining transcription factor Gata3. We found that Zfp281 interacts with Gata3 and is recruited to Gata3 genomic binding sites at loci encoding Thpok and TH2 cytokines. Thus, Zfp148 and Zfp281 collaborate with Gata3 to promote CD4+ T cell development and TH2 cell responses.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Linfócitos T CD4-Positivos Limite: Animals Idioma: En Revista: Sci Immunol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Linfócitos T CD4-Positivos Limite: Animals Idioma: En Revista: Sci Immunol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos